List of variants in gene DNAJC6 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001256864.2(DNAJC6):c.1320A>T (p.Thr440=)	rs142136708	0.00462
NM_001256864.2(DNAJC6):c.745A>G (p.Ile249Val)	rs149588872	0.00357
NM_001256864.2(DNAJC6):c.1182A>G (p.Leu394=)	rs148145327	0.00015
NM_001256864.2(DNAJC6):c.264G>A (p.Gly88=)	rs139946043	0.00005
NM_001256864.2(DNAJC6):c.2526A>G (p.Leu842=)	rs753691766	0.00004
NM_001256864.2(DNAJC6):c.144G>T (p.Arg48=)	rs779540362	0.00003
NM_001256864.2(DNAJC6):c.2061C>T (p.Asn687=)
NM_001256864.2(DNAJC6):c.2373G>A (p.Gln791=)
NM_001256864.2(DNAJC6):c.261A>C (p.Ala87=)
NM_001256864.2(DNAJC6):c.2886A>G (p.Glu962=)

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